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Human Molecular Genetics|June 14, 2015
Mitochondrial energetic defects in muscle and brain of a Hmbs-/- mouse model of acute intermittent porphyriaChadi Homedan, Caroline Schmitt, Jihane Laafi, et al.
Life (Basel, Switzerland)|January 23, 2024
Severe Perinatal Presentations of Günther's Disease: Series of 20 Cases and PerspectivesClaire Goudet, Cécile Ged, Audrey Petit, et al.
Maternal & Child Nutrition|May 4, 2017
Very low prevalence of iron deficiency among young French children: A national cross-sectional hospital-based surveyAnne-Sylvia Sacri, Serge Hercberg, Laurent Gouya, et al.
JACC. Advances|June 18, 2025
Simple Renal Cysts in Marfan Syndrome: Prevalence and Association With Aortic EventsClaire Bouleti, Noemie Tence, Raphael Thuillier, et al.
Frontiers in Cardiovascular Medicine|August 22, 2017
Erythrocyte Efferocytosis by the Arterial Wall Promotes Oxidation in Early-Stage Atheroma in HumansSandrine Delbosc, Richard Graham Bayles, Jamila Laschet, et al.
Clinical Nutrition (Edinburgh, Scotland)|June 9, 2020
Young children formula consumption and iron deficiency at 24 months in the general population: A national-level studyAnne-Sylvia Sacri, Alain Bocquet, Mariane de Montalembert, et al.
Blood|July 18, 2020
Iron chelation rescues hemolytic anemia and skin photosensitivity in congenital erythropoietic porphyriaJean-Marc Blouin, Cécile Ged, Magalie Lalanne, et al.
Human Molecular Genetics|September 15, 2005
Mutations in human CPO gene predict clinical expression of either hepatic hereditary coproporphyria or erythropoietic harderoporphyriaCaroline Schmitt, Laurent Gouya, Eva Malonova, et al.
The Journal of Pediatrics|April 9, 2021
Clinical Prediction of Iron Deficiency at Age 2 Years: A National Cross-sectional Study in FranceClaire Guivarch, Anne-Sylvia Sacri, Corinne Levy, et al.
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